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Items: 1 to 20 of 39

1.
The E3 ligase Poe promotes Pericentrin degradation
Brian J. Galletta, Ramya Varadarajan, Carey J. Fagerstrom, Bing Yang, Karen Plevock Haase, Katherine McJunkin, Nasser M. Rusan
Mol Biol Cell. 2023 Aug 1; 34(9): br15. Published online 2023 Aug 1. doi: 10.1091/mbc.E22-11-0534
PMCID:
PMC10398894
AbstractArticlePDF–4.7M
2.
Expanded directly binds conserved regions of Fat to restrain growth via the Hippo pathway
Alexander D. Fulford, Leonie Enderle, Jannette Rusch, Didier Hodzic, Maxine V. Holder, Alex Earl, Robin Hyunseo Oh, Nicolas Tapon, Helen McNeill
J Cell Biol. 2023 May 1; 222(5): e202204059. Published online 2023 Apr 18. doi: 10.1083/jcb.202204059
PMCID:
PMC10120405
AbstractArticlePDF–6.6M
3.
Next-generation large-scale binary protein interaction network for Drosophila melanogaster
Hong-Wen Tang, Kerstin Spirohn, Yanhui Hu, Tong Hao, István A. Kovács, Yue Gao, Richard Binari, Donghui Yang-Zhou, Kenneth H. Wan, Joel S. Bader, Dawit Balcha, Wenting Bian, Benjamin W. Booth, Atina G. Coté, Steffi de Rouck, Alice Desbuleux, Kah Yong Goh, Dae-Kyum Kim, Jennifer J. Knapp, Wen Xing Lee, Irma Lemmens, Cathleen Li, Mian Li, Roujia Li, Hyobin Julianne Lim, Yifang Liu, Katja Luck, Dylan Markey, Carl Pollis, Sudharshan Rangarajan, Jonathan Rodiger, Sadie Schlabach, Yun Shen, Dayag Sheykhkarimli, Bridget TeeKing, Frederick P. Roth, Jan Tavernier, Michael A. Calderwood, David E. Hill, Susan E. Celniker, Marc Vidal, Norbert Perrimon, Stephanie E. Mohr
Nat Commun. 2023; 14: 2162. Published online 2023 Apr 15. doi: 10.1038/s41467-023-37876-0
PMCID:
PMC10105736
AbstractArticlePDF–3.2M
4.
Distinct mechanisms of planar polarization by the core and Fat-Dachsous planar polarity pathways in the Drosophila wing
Amy Brittle, Samantha J. Warrington, Helen Strutt, Elizabeth Manning, Su Ee Tan, David Strutt
Cell Rep. 2022 Sep 27; 40(13): 111419. Published online 2022 Sep 27. doi: 10.1016/j.celrep.2022.111419
PMCID:
PMC9631118
AbstractArticle
5.
Emerging Mechanisms of Growth and Patterning Regulation by Dachsous and Fat Protocadherins
Artem Gridnev, Jyoti R. Misra
Front Cell Dev Biol. 2022; 10: 842593. Published online 2022 Mar 16. doi: 10.3389/fcell.2022.842593
PMCID:
PMC8967653
AbstractArticlePDF–1.1M
6.
Genome-wide phenotypic RNAi screen in the Drosophila wing: phenotypic description of functional classes
Ana López-Varea, Patricia Vega-Cuesta, Ana Ruiz-Gómez, Cristina M Ostalé, Cristina Molnar, Covadonga F Hevia, Mercedes Martín, Maria F Organista, Jesus de Celis, Joaquín Culí, Nuria Esteban, Jose F de Celis
G3 (Bethesda) 2021 Dec; 11(12): jkab349. Published online 2021 Oct 2. doi: 10.1093/g3journal/jkab349
PMCID:
PMC8664486
AbstractArticlePDF–3.1M
7.
Elucidate growth control mechanisms using reconstructed spatiotemporal distributions of signaling events
Hao Zhu
Comput Struct Biotechnol J. 2021; 19: 3618–3627. Published online 2021 Jun 18. doi: 10.1016/j.csbj.2021.06.019
PMCID:
PMC8249872
AbstractArticlePDF–4.1M
8.
Negative feedback couples Hippo pathway activation with Kibra degradation independent of Yorkie-mediated transcription
Sherzod A Tokamov, Ting Su, Anne Ullyot, Richard G Fehon
eLife. 2021; 10: e62326. Published online 2021 Feb 8. doi: 10.7554/eLife.62326
PMCID:
PMC7895526
AbstractArticlePDF–10M
9.
CRISPR-based modular assembly of a UAS-cDNA/ORF plasmid library for more than 5500 Drosophila genes conserved in humans
Ping Wei, Wen Xue, Yun Zhao, Guang Ning, Jiwu Wang
Genome Res. 2020 Jan; 30(1): 95–106. doi: 10.1101/gr.250811.119
PMCID:
PMC6961578
AbstractArticlePDF–3.6M
10.
Landscape and evolution of tissue-specific alternative polyadenylation across Drosophila species
Piero Sanfilippo, Jiayu Wen, Eric C. Lai
Genome Biol. 2017; 18: 229. Published online 2017 Nov 30. doi: 10.1186/s13059-017-1358-0
PMCID:
PMC5707805
AbstractArticlePDF–3.2M
11.
Transcription elongation rate has a tissue-specific impact on alternative cleavage and polyadenylation in Drosophila melanogaster
Xiaochuan Liu, Jaime Freitas, Dinghai Zheng, Marta S. Oliveira, Mainul Hoque, Torcato Martins, Telmo Henriques, Bin Tian, Alexandra Moreira
RNA. 2017 Dec; 23(12): 1807–1816. doi: 10.1261/rna.062661.117
PMCID:
PMC5689002
AbstractArticlePDF–4.0M
12.
The palmitoyltransferase Approximated promotes growth via the Hippo pathway by palmitoylation of Fat
Hitoshi Matakatsu, Seth S. Blair, Richard G. Fehon
J Cell Biol. 2017 Jan 2; 216(1): 265–277. doi: 10.1083/jcb.201609094
PMCID:
PMC5223609
AbstractArticlePDF–3.3M
13.
The novel SH3 domain protein Dlish/CG10933 mediates fat signaling in Drosophila by binding and regulating Dachs
Yifei Zhang, Xing Wang, Hitoshi Matakatsu, Richard Fehon, Seth S Blair
eLife. 2016; 5: e16624. Published online 2016 Oct 3. doi: 10.7554/eLife.16624
Correction in:
eLife. 2016; 5: e22672.
PMCID:
PMC5047748
AbstractArticlePDF–9.8M
14.
mRNA-Associated Processes and Their Influence on Exon-Intron Structure in Drosophila melanogaster
Gildas Lepennetier, Francesco Catania
G3 (Bethesda) 2016 Jun; 6(6): 1617–1626. Published online 2016 Mar 28. doi: 10.1534/g3.116.029231
PMCID:
PMC4889658
AbstractArticlePDF–1.5M
15.
A genetic interaction map of cell cycle regulators
Maximilian Billmann, Thomas Horn, Bernd Fischer, Thomas Sandmann, Wolfgang Huber, Michael Boutros
Mol Biol Cell. 2016 Apr 15; 27(8): 1397–1407. doi: 10.1091/mbc.E15-07-0467
PMCID:
PMC4831891
AbstractArticlePDF–4.0M
16.
Genes conserved in bilaterians but jointly lost with Myc during nematode evolution are enriched in cell proliferation and cell migration functions
Albert J. Erives
Dev Genes Evol. 2015; 225(5): 259–273. Published online 2015 Jul 15. doi: 10.1007/s00427-015-0508-1
PMCID:
PMC4568025
AbstractArticlePDF–2.8M
17.
Gene Model Annotations for Drosophila melanogaster: The Rule-Benders
Madeline A. Crosby, L. Sian Gramates, Gilberto dos Santos, Beverley B. Matthews, Susan E. St. Pierre, Pinglei Zhou, Andrew J. Schroeder, Kathleen Falls, David B. Emmert, Susan M. Russo, William M. Gelbart, the FlyBase Consortium
G3 (Bethesda) 2015 Aug; 5(8): 1737–1749. Published online 2015 Jun 24. doi: 10.1534/g3.115.018937
PMCID:
PMC4528330
AbstractArticlePDF–2.2M
18.
Gene Model Annotations for Drosophila melanogaster: Impact of High-Throughput Data
Beverley B. Matthews, Gilberto dos Santos, Madeline A. Crosby, David B. Emmert, Susan E. St. Pierre, L. Sian Gramates, Pinglei Zhou, Andrew J. Schroeder, Kathleen Falls, Victor Strelets, Susan M. Russo, William M. Gelbart, the FlyBase Consortium
G3 (Bethesda) 2015 Aug; 5(8): 1721–1736. Published online 2015 Jun 24. doi: 10.1534/g3.115.018929
PMCID:
PMC4528329
AbstractArticlePDF–4.9M
19.
Control of Organ Growth by Patterning and Hippo Signaling in Drosophila
Kenneth D. Irvine, Kieran F. Harvey
Cold Spring Harb Perspect Biol. 2015 Jun; 7(6): a019224. doi: 10.1101/cshperspect.a019224
PMCID:
PMC4448604
AbstractArticlePDF–873K
20.
The Release 6 reference sequence of the Drosophila melanogaster genome
Roger A. Hoskins, Joseph W. Carlson, Kenneth H. Wan, Soo Park, Ivonne Mendez, Samuel E. Galle, Benjamin W. Booth, Barret D. Pfeiffer, Reed A. George, Robert Svirskas, Martin Krzywinski, Jacqueline Schein, Maria Carmela Accardo, Elisabetta Damia, Giovanni Messina, María Méndez-Lago, Beatriz de Pablos, Olga V. Demakova, Evgeniya N. Andreyeva, Lidiya V. Boldyreva, Marco Marra, A. Bernardo Carvalho, Patrizio Dimitri, Alfredo Villasante, Igor F. Zhimulev, Gerald M. Rubin, Gary H. Karpen, Susan E. Celniker
Genome Res. 2015 Mar; 25(3): 445–458. doi: 10.1101/gr.185579.114
PMCID:
PMC4352887
AbstractArticlePDF–1022K

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